FDA 510(k) Applications Submitted by HDC CORP.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K953300 |
07/14/1995 |
V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER |
HDC CORP. |
| K010425 |
02/13/2001 |
EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) |
HDC CORP. |
| K071875 |
07/06/2007 |
V-CATH POLY PICC |
HDC CORP. |
| K032404 |
08/04/2003 |
SELDINGER SAFETY NEEDLE INTRODUCER |
HDC CORP. |
| K022752 |
08/19/2002 |
PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15 |
HDC CORP. |
| K002770 |
09/06/2000 |
IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL 700-08-10,700-08-11,700-08-12,700-08-15,700-08-16,735-08-10 |
HDC CORP. |
| K023342 |
10/07/2002 |
NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BG |
HDC CORP. |
| K033853 |
12/11/2003 |
MODIFICATION TO V-CATH POLY PICC |
HDC CORP. |
| K964966 |
12/11/1996 |
V-CATH |
HDC CORP. |
| K994059 |
11/29/1999 |
CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07 |
HDC CORP. |
| K983409 |
09/28/1998 |
V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) SEE APPENDIX 1 |
HDC CORP. |
| K983916 |
11/03/1998 |
V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) |
HDC CORP. |
| K022099 |
06/27/2002 |
SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'S |
HDC CORP. |
| K983119 |
09/08/1998 |
ENTERO-TEST HP, MODEL #102-01 |
HDC CORP. |
|
|
